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崔霞, 邹明强, 胡秀丽, 韩博, 金涌. 氢醌对体外培养鼠角质形成细胞毒性作用[J]. 中国公共卫生, 2008, 24(4): 467-468. DOI: 10.11847/zgggws2008-24-04-49
引用本文: 崔霞, 邹明强, 胡秀丽, 韩博, 金涌. 氢醌对体外培养鼠角质形成细胞毒性作用[J]. 中国公共卫生, 2008, 24(4): 467-468. DOI: 10.11847/zgggws2008-24-04-49
CUI Xia, ZOU Ming-qiang, HU Xiu-li, . Toxic effects of hydroquinone on rat epidermal keratinocytes[J]. Chinese Journal of Public Health, 2008, 24(4): 467-468. DOI: 10.11847/zgggws2008-24-04-49
Citation: CUI Xia, ZOU Ming-qiang, HU Xiu-li, . Toxic effects of hydroquinone on rat epidermal keratinocytes[J]. Chinese Journal of Public Health, 2008, 24(4): 467-468. DOI: 10.11847/zgggws2008-24-04-49

氢醌对体外培养鼠角质形成细胞毒性作用

Toxic effects of hydroquinone on rat epidermal keratinocytes

  • 摘要: 目的 研究氢醌(Hydroquinone,HQ)对体外培养正常鼠表皮角质形成细胞的毒性作用。方法 用0,1,2.5,5,10和25μg/ml的氢醌处理鼠角质形成细胞,检测氢醌对角质形成细胞的增殖抑制率、乳酸脱氢酶(LDH)释放率、细胞中活性氧(ROS)水平、丙二醛(MDA)含量,并对超氧化物歧化酶(SOD)和还原性谷胱甘肽过氧化酶(GSH-Px)的活力进行测定。结果 氢醌可引起角质形成细胞活力剂量-时间依赖性降低;角质形成细胞用0,1,2.5,5,10和25μg/ml氢醌处理4,8,12,24 h后,LDH释放率呈明显的时间-剂量-反应关系;同样剂量的氢醌处理角质形成细胞,12 h后可引起ROS、MDA含量呈浓度依赖性增加(最低浓度为5μg/ml),而SOD及GSH-Px活力呈浓度依赖性抑制(最低浓度为2.5μg/ml),与对照组比较差异均有统计学意义(P<0.05,P<0.01)。结论 在体外培养条件下,氢醌可通过脂质过氧化和氧化应激对鼠角质形成细胞产生明显的毒性作用。

     

    Abstract: Objective To study the cytotoxicity of hydroquinone(HQ)on normal ratepidermal keratinocytes in vitro.Methods Keratinocytes were treated with HQ of 0,1,215,5,10 and 25μg/ml.The cell proliferation,lactate dehydrogenase (LDH)release,reactive oxygen species(ROS)level,malondialdehyde(MDA)content and activity of glutathione peroxide (GSH-Px)and superoxide dismutase(SOD)in keratinocyte were detected respectively.Results HQ could induce a dose and time-dependent decrease in cell viability.A time and concentration-dependent release of LDH was observed after cells were exposed to 0,1,215,5,10 and 25μg/ml HQ.When the same concentration HQ treated keratinocytes for 12 h,HQ also induced an increase of ROS intensity and MDA content,while an inhibition of SOD and GSH-Px activity in a concentration dependent manner.The lowest concentration were 5μg/ml and 215μg/ml,respectively.Compared withthe control group,the variance was significant(P<0.05,P<0.01).Conclusion The results suggest thathQ could induce cytotoxicity to cultured rat epidermal keratinocyte in vitro,which was associated withlipid peroxidation and oxidative stress.

     

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